BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Ti-Diagon Oblique TLIF

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    External Fixation

    FDA UDI
    Life Spine, Inc.·00190837033972·Short Drill Sleeve

    GRAVILAX TRACTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    BD FACS SAMPLE PREP ASSISTANT III (SPA III)

    FDA 510(k)
    FDA Class 2 ·Hematology

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 19, 2022

    PLUM A+ DRIVER ED 2

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 10, 2013

    LIGASURE PRECISE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·June 16, 2011

    WALLSTENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code FGE·September 23, 2008

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·September 15, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FCG·June 28, 2023

    PUSHING CATHETER

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·March 5, 2021